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Disease Spirochete

Artem S. Rogovskyy1, Troy Bankhead1,2*

1Department of Veterinary Microbiology and Pathology, Washington State University, Pullman, Washington, United States of America,2Paul G. Allen School for Global Animal Health, Washington State University, Pullman, Washington, United States of America

Abstract

Many pathogens make use of antigenic variation as a way to evade the host immune response. A key mechanism for immune evasion and persistent infection by the Lyme disease spirochete,Borrelia burgdorferi, is antigenic variation of the VlsE surface protein. Recombination results in changes in the VlsE surface protein that prevent recognition by VlsE-specific antibodies in the infected host. Despite the presence of a substantial number of additional proteins residing on the bacterial surface, VlsE is the only known antigen that exhibits ongoing variation of its surface epitopes. This suggests that B.

burgdorferi may utilize a VlsE-mediated system for immune avoidance of its surface antigens. To address this, the

requirement of VlsE for host reinfection by the Lyme disease pathogen was investigated. Host-adapted wild type and VlsE mutant spirochetes were used to reinfect immunocompetent mice that had naturally cleared an infection with a VlsE-deficient clone. Our results demonstrate that variable VlsE is necessary for reinfection byB. burgdorferi, and this ability is directly related to evasion of the host antibody response. Moreover, the data presented here raise the possibility that VlsE prevents recognition ofB. burgdorferisurface antigens from host antibodies. Overall, our findings represent a significant advance in our knowledge of immune evasion byB. burgdorferi, and provide insight to the possible mechanisms involved in VlsE-mediated immune avoidance.

Citation:Rogovskyy AS, Bankhead T (2013) Variable VlsE Is Critical for Host Reinfection by the Lyme Disease Spirochete. PLoS ONE 8(4): e61226. doi:10.1371/ journal.pone.0061226

Editor:Brian Stevenson, University of Kentucky College of Medicine, United States of America

ReceivedDecember 17, 2012;AcceptedMarch 8, 2013;PublishedApril 8, 2013

Copyright:ß2013 Rogovskyy and Bankhead. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Funding:This work was supported by an intramural grant from the College of Veterinary Medicine, Washington State University. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests:The authors have declared that no competing interests exist.

* E-mail: tbankhead@vetmed.wsu.edu

Introduction

Borrelia burgdorferi is the causative agent of the multisystem disease known as Lyme borreliosis, which is currently the most prevalent vector-borne disease in North America [1,2,3]. Infection with this spirochete can be severely debilitating to both animals and humans, resulting in long-term manifestations including arthritis, carditis, and neurological problems [4]. Although persistent infection can last from months to years due to avoidance of the host immune response by the pathogen, early infection can usually be cleared with antibiotic treatment. Surprisingly, reinfec-tion occurs fairly regularly in post-treatment patients that have successfully cleared initial infection, suggesting that individuals treated for early Lyme disease continue to remain at risk for reinfection [5,6,7,8,9,10,11,12,13]. The incidence of reinfection has been shown to be as high as 15% over a five-year study period (a rate of 3% per year), and clinical manifestations seem to be identical to those of initial infection [6].

Key to the successful immune evasion tactics ofB. burgdorferiis recombination at thevlslocus located at the right telomeric end of a 28-kilobase linear plasmid (lp28-1) in the B31 strain [14,15,16]. Recombinational switching at the vls locus results in sequence variation of the surface lipoprotein, VlsE, which alters its antigenic properties and allows the spirochete to evade the host’s antibody-mediated response [16,17,18]. Evidence for the role of the vls system in immune avoidance was first provided by studies involving thevls-resident plasmid, lp28-1 [19,20]. Clones lacking

lp28-1 were shown to exhibit an intermediate infectivity pheno-type whereby these spirochetes were able to disseminate to tissue sites but were unable to persist in the murine host. These same clones are capable of long-term survival in severe-combined immunodeficient (SCID) mice that lack an effective antibody response [21,22]. lp28-1-deficient isolates also grow normally in a dialysis membrane chamber implanted in the peritoneal cavity of rats, where exposure to either antibodies or immune cells is restricted [22]. Moreover, immunocompetent mice infected with an lp28-1-deficient clone complemented with only thevlsE gene (sans the vls silent cassettes) are able to clear infection, demon-strating that it is not the mere presence of VlsE that provides the capacity for persistent infection, but rather the ability to undergo vls recombination to produce VlsE variants [23]. Finally, spirochetes that lack only thevlslocus due to telomere-mediated removal are completely cleared from immunocompetent C3H mice by 21 days post infection [24], confirming the hypothesis that vls recombination functions to evade the humoral immune response in the mouse host [14,16,25,26].

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antigenic variation process [16,17,18,26,30,31]. A role for the VlsE protein other than antigenic variation is not currently known, but it has been proposed that the protein might function in other forms of immune evasion [32,33].

Although a number of other surface proteins exist that are immunogenic, VlsE is the only known B. burgdorferiantigen that exhibits active variation of its surface epitopes. This fact may suggest thatB. burgdorferiuses a specialized VlsE-mediated system for immune avoidance of its surface antigens. Many pathogens utilize their antigenically variable proteins in a number of ways as an evasion strategy, and models have been suggested for how VlsE might become the primary target for the host immune response [24,33]. One possibility is that VlsE may act as a shield to obscure the epitopes of other surface antigens. A precedent for this type of interaction has been demonstrated in studies with theB. burgdorferi protein P66, in which the protein is protected from antibodies and proteolytic cleavage in spirochetes expressing high levels of the outer surface protein, OspA [34]. It has also been proposed that VlsE might be a T-cell independent antigen that could directly stimulate B cells [24,33]. The resulting humoral response generated by VlsE may serve to override antibody production against other potential surface antigens in such a way that antibodies to non-VlsE surface antigens are produced at insuffi-cient titers in order to clear theBorreliainfection.

To date, a link between the capacity ofB. burgdorferi for host reinfection and the antigenically variable VlsE protein has not been examined in detail. In the current study, we utilized host-adapted wild type and VlsE-deficient clones to infect mice with an active humoral response to B. burgdorferi in order to address the question of VlsE-mediated immune evasion. We report for the first time that variable VlsE is critical for establishing murine reinfection by B. burgdorferi. Moreover, our findings suggest that host reinfection occurs through escape of non-VlsE surface antigens from humoral immune surveillance, possibly through a VlsE-dependent mechanism.

Results

Generation and characterization of aB. burgdorferi

mutant expressing non-variable VlsE

A recent study attempted to address the role of VlsE in host reinfection through the use of sera from infected mice [24], however the results from this study were ultimately inconclusive. The inherent problem with these experiments is that in vitro-cultured B. burgdorferi were utilized, which have been shown to have a 32-fold reduction in VlsE expression levels relative to those measured during murine infection [35]. Unlike these highly susceptible in vitro-grown spirochetes, B. burgdorferi that have adapted within either the feeding tick or animal host have been demonstrated to be relatively invulnerable to the protective effects of immune sera [36,37]. For this reason, we chose to use host-adapted spirochetes in order to re-examine whether reinfection of a mouse host by B. burgdorferirequires the presence of the VlsE protein. To obtain host-adapted spirochetes for this study, ear tissues from severe combined immunodeficient (SCID) mice infected with either wild-type orvlsE mutantB. burgdorferi clones were harvested. These ear tissues containing host-adapted B. burgdorferi were then transplanted via subcutaneous incisions in order to infect or reinfect mice.

In order to determine whether variable or static VlsE could provide a capacity for reinfection, we first set out to generate aB. burgdorferimutant clone containing a non-switchablevlsEgene on lp28-1. To generate this ‘‘static’’ VlsE mutant clone (sVlsE), we utilized a targeted deletion strategy that resulted in the

replace-ment of the entirevlslocus with a copy of only thevlsEgene and native basal promoter. As shown in Figure 1A, the targeted deletion plasmid contains a kanamycin-resistant cassette (kan), a replicated telomere (rtel), and a target DNA sequence identical to a 1.2 kb stretch of lp28-1 just upstream of thevlslocus in the B31-A3 wild type clone [38]. Homologous recombination at the DNA target sequence followed by telomere resolution by endogenous ResT leads to deletion of the 15 silent cassettes and nativevlsE expression site, which is replaced by the kangene and a newly introduced copy ofvlsEwith its native promoter. ThisvlsEgene is unable to undergovlsrecombination due to the absence of the 15 silent cassettes, and thereforeB. burgdorfericlones carrying this non-switchablevlsEwill only express a single static version of the VlsE lipoprotein.

Overall, ten kanamycin-resistant transformants were recovered and PCR screened for the presence of thekangene. Several clones were selected and further analyzed by PCR to ensure retention of B. burgdorferiplasmids, including those essential for infectivity [39]. One sVlsE clone that contained the full plasmid profile, with the exception of cp9, was chosen for further analyses (Table 1). The cp9 plasmid is normally absent from the parental B31-A3 wild type clone, and is not necessary for infection or pathogenesis [38]. The truncation of lp28-1 was confirmed by field inversion gel analysis (Figure 1B) and verified by Southern blot (data not shown). Expression and surface localization of VlsE by the sVlsE clone was confirmed by surface proteolysis via Western blot analysis (Figure 2), which showed lower overall expression than that of the wild type (WT). As shown in Table 2, the sVlsE clone was found to be infectious in both immunocompetent C3H/ HeNHsd (C3H) and immunodeficient SCID mice. Similar to published studies involving previously characterized non-switch-able VlsE mutants [16,24], the sVlsE clone was not non-switch-able to establish persistent infection in immunocompetent C3H mice, but could maintain long-term infection in SCID mice. Similarly and consistent with a previous study, a clone lacking the entirevlslocus (DVlsE) exhibited persistent infection only in immunodeficient SCID animals [24].

Finally, in order to confirm the infectivity of host-adapted B. burgdorferi clones to be used for this study, SCID ear tissues containing either theDVlsE mutant clone, sVlsE mutant clone, or WT control were transplanted into naı¨ve C3H mice. As shown in Table 3, blood collected and cultured for spirochetes at day 7 post infection demonstrated that all mice had been successfully infected with each of the host-adapted B. burgdorferi clones. Ear tissues collected at days 14, 21 and 28 post infection showed that mice infected with WT were persistently infected, while all mice infected with either of the VlsE-mutant clones were cleared of infection by day 21 post infection. With an infectious clone expressing a static form of VlsE now generated and the infectivity of host-adapted clones verified, the requirement of VlsE for host reinfection was assessed.

Variable VlsE is required for host reinfection byB. burgdorferi

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into three groups, and then challenged with either host-adapted WT, DVlsE or sVlsE via tissue transplantation to assay for the ability to reinfect mice (see Figure 3).

The results from this experiment showed that host-adapted WT was able to reinfect all mice that had cleared DVlsE-induced infection (4 out of 4) as determined by positive cultures of blood samples drawn at day 7 post transplantation (groupDVlsE-WT; Table 4). Moreover, ear tissues obtained from all animals at day 21 and 28 post transplantation were culture positive for the WT clone, indicating that the mice became persistently infected. WT spirochetes were also cultured from heart, bladder and joint tissues harvested at day 28 post transplantation, demonstrating tissue dissemination. In contrast, the DVlsE clone was not able to reinfect any mice originally infected with and cleared of this same clone (groupDVlsE-DVlsE; Table 4). Immunoblots of WT, sVlsE, or DVlsE whole-cell lysates that were blotted withB. burgdorferi clone-specific immune sera collected at day 28 post infection displayed similar antibody response patterns (Figure 4). Thus, the difference in the ability ofB. burgdorfericlones to reinfect does not seem to be attributed to any noticeable difference in the total Borrelia-specific antibody response. Together, these results suggest that the immune response of these mice to non-VlsE surface antigens can sufficiently block reinfection by aB. burgdorfericlone lacking VlsE, but is unable to prevent reinfection by the WT clone containing VlsE. However, the sVlsE clone was not recovered from any mouse (groupDVlsE-sVlsE; Table 4) that had previously

cleared infection with the DVlsE clone, suggesting that the presence of a non-switchable form of VlsE in these spirochetes does not provide the capacity for reinfection. Thus, this finding may indicate that it is not the mere presence of VlsE that is necessary to allow host reinfection, but rather a variable form of the protein.

In order to assess whether mice exposed toB. burgdorfericlones expressing a static form of VlsE could mount an immune response capable of preventing reinfection, a similar experiment was conducted with C3H mice that had cleared sVlsE-induced infection. As shown in Table 4, WT spirochetes were able to successfully reinfect mice originally infected with and cleared of the sVlsE clone (sVlsE-WT). Conversely, these mice were not reinfected byDVlsE (group sVlsE-DVlsE; Table 4), suggesting that antibodies against non-VlsE surface antigens were generated during initial infection with the sVlsE clone. As expected, mice infected with sVlsE were resistant to reinfection with the host-adapted sVlsE clone (sVlsE-sVlsE; Table 4), presumably due to a preexisting immune response developed specifically against the static form of VlsE expressed in this mutant clone. Taken together, Figure 1. Generation ofB. burgdorferimutant with non-switchablevlsE in cis.A) Schematic illustrating the replacement of thevlslocus with a non-switchablevlsEgene. The targeted deletion construct, pAR2, is inserted into lp28-1 via homologous recombination at the target DNA sequence. Following telomere resolution by endogenous ResT, the right end of lp28-1 containing the 15 silent cassettes andvlsEexpression site is deleted. The resultant truncated plasmid, lp28-1Dvls::vlsE, containedvlsEwith native basal promoter (denoted asp) and kanamycin-resistant gene (kan). The four leftward facing arrows represent the genes required for autonomous replication of lp28-1. Telomere regions and replicated telomere (rtel) are indicated as hatched regions. B) Analysis of the lp28-1Dvls::vlsEconstruct by field inversion gel electrophoresis. Genomic DNA from WT,DVlsE, and sVlsE are shown in lanes 1, 2, and 3, respectively. Positions of lp28-1Dvls::vlsE and lp28-1Dvlsare shown by the arrowhead and angled line, respectively. The positions of DNA markers are indicated on the left.

doi:10.1371/journal.pone.0061226.g001

Figure 2. Expression and surface localization of VlsE by B. burgdorfericlones.Intact spirochetes were treated with or without proteinase K for 40 min followed by SDS-polyacrylamide gel electro-phoresis (108cells/lane) and Western blotting. Two identical blots were

processed with anti-VlsE or anti-FlaB antibodies. Lanes 1, 3, and 5 show that VlsE is only expressed by the WT and sVlsE clones, but not by the DVlsE clone. Treatment with proteinase K dramatically reduced VlsE immunostaining for the WT and sVlsE clones, but had no effect on levels of the periplasmic protein, FlaB. A non-specific band that remains after proteinase K digestion can also be seen in the anti-VlsE blot. doi:10.1371/journal.pone.0061226.g002

Table 1.Borrelia burgdorfericlones used in the study.

B. burgdorferi B31 clone

Missing

plasmid(s) vls2-16a vlsE Reference

A3 (WT) cp9 + + [38]

A3 lp28-1Dvls(DVlsE) cp9 2 2 [24]

A3 lp28-1Dvls::vlsE(sVlsE) cp9 2 + This study

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the above experiments demonstrate for the first time that variable VlsE is absolutely required for B. burgdorferi to reinfect both immunologically VlsE-naı¨ve and VlsE-exposed mice.

Variable VlsE is sufficient for escape fromBorrelia-specific immune sera

Results from the above reinfection experiments suggest that variable VlsE is capable of providing protection against anti-Borreliahost immunity, specifically the adaptive immune response. To address whether variable VlsE prevented recognition of non-VlsE surface antigens by host Borrelia-specific antibodies, we designed a passive transfer experiment using SCID mice as a model. The experimental scheme included six groups of SCID mice as shown in Figure 5. Mice in groups I, II, and III received immune sera obtained from immunocompetent C3H mice that had clearedDVlsE-induced infection by day 21 post infection, and thus contained antibodies generated against variousB. burgdorferi surface proteins except VlsE. Immunized SCID mice of groups I, II, and III were challenged with either host-adapted WT,DVlsE, or sVlsE spirochetes, respectively. At day 7 post transplantation, blood, heart, ear, bladder and joint tissues were harvested to determine whether the immune sera prevented infection. As expected, mice were successfully challenged by the WT clone despite the presence of DVlsE-specific immune sera (group I; Table 5). In contrast, theDVlsE clone was not detected in tissues of any mice, indicating that host-adapted spirochetes lacking the VlsE protein are susceptible to DVlsE-specific immune sera treatment (group II; Table 5). Consistent with the reinfection findings, DVlsE-specific sera also prevented host-adapted sVlsE infection in 3 out of 3 mice, suggesting that static VlsE does not allowB. burgdorferito evadeBorrelia-specific host antibodies (group III; Table 5).

Immune sera generated from immunocompetent mice infected with the WT clone (WT-specific sera) also prevented challenge with the VlsE-deficient DVlsE clone (group IV; Table 5), suggesting that VlsE does not suppress production of non-VlsE specific antibodies in the course of an adaptive immune response. Expectedly, mice that received preimmune sera were successfully infected with either theDVlsE or sVlsE clone (groups V and VI; Table 5), demonstrating that these clones were fully capable of infecting mice. Together, these data support the findings of our reinfection experiments, emphasizing the importance of variable VlsE for B. burgdorferi evasion of the host adaptive immune response toB. burgdorferisurface antigens.

Static VlsE-expressingB. burgdorferican successfully resist immune sera treatment after established infection

One possible explanation for the inability of the sVlsE clone to reinfect VlsE-naı¨ve mice is a low infectious dose of host-adapted spirochetes expressing the static form of VlsE. This could arise due to spontaneous loss of the lp28-1Dvls::vlsE plasmid during the three-week infection period in SCID donor mice prior to tissue transplantation. Indeed, recent work in our lab has found that a portion of spirochetes recovered from tissues of SCID mice infected with the sVlsE clone no longer retain the lp28-1 plasmid (Rogovskyy and Bankhead, unpublished results). To account for the possibility of a low infectious dose of static VlsE-expressing clones, we allowed tissue-transplanted spirochetes to propagatein vivo for four days prior to immune sera treatment in order to increase the number of spirochetes carrying lp28-1Dvls::vlsE during initial infection. Specifically, SCID mice were infected with either the host-adaptedDVlsE or sVlsE clone (groups A and C; Table 6), and after 4 days post infection these mice were given immune sera obtained from immunocompetent mice that had cleared infection withDVlsE (DVlsE-specific sera). Infection was Table 2.Infectivity ofin vitro-grown VlsE mutants in naı¨ve SCID and C3H mice.

Tissue collected (at

day post infection) Naı¨ve SCID mice infected with Naı¨ve C3H mice infected with

WT DVlsE sVlsE WT DVlsE sVlsE

Blood (day 7) 3/3a 3/3 3/3 4/4 5/5 5/5

Ear (day 14) 3/3 3/3 3/3 3/4 3/5 4/5

Ear (day 21) 3/3 3/3 3/3 4/4 0/5 0/5

Ear (day 28) 3/3 3/3 3/3 4/4 0/5 0/5

aValues listed correspond to numbers of cultures positive/numbers tested. doi:10.1371/journal.pone.0061226.t002

Table 3.Infectivity of host-adapted VlsE mutants in naı¨ve C3H mice.

Tissue collected (at day post

infection) Naı¨ve C3H mice infected via tissue transplantation witha

ha WTb ha

DVlsE ha sVlsE

Blood (day 7) 3/3 3/3 3/3

Ear (day 14) 3/3 1/3 2/3

Ear (day 21) 3/3 0/3 0/3

Ear (day 28) 3/3 0/3 0/3

aValues listed correspond to numbers of cultures positive/numbers tested. bha denotes host-adapted clone.

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then monitored by culturing blood collected at day 3 and 7 post sera treatment.

The results show that DVlsE-specific immune sera treatment was able to successfully clear infection with host-adaptedDVlsE spirochetes (group A; Table 6), verifying the bactericidal efficacy of the immune sera. In contrast, the sVlsE clone was able to survive in SCID mice despite the presence ofDVlsE-specific immune sera, suggesting that these mutant spirochetes expressing static VlsE can evade host antibodies (group C; Table 6). The sVlsE isolates obtained from positive blood cultures were kanamycin resistant and PCR positive for vlsE, indicating that the lp28-1Dvls::vlsE plasmid was retained in these recovered clones (data not shown). All mice infected with host-adapted DVlsE or sVlsE and given preimmune sera remained infected at day 3 and 7 post sera treatment, demonstrating the viability and infectivity of these clones under the experimental conditions (groups B and D; Table 6). Overall, these data suggest that static VlsE can provide some measure of immune avoidance for non-VlsE surface antigens, but only after infection is established.

Figure 3. Experimental design to assay for a VlsE requirement for host reinfection.C3H mice were initially infected within vitro-grown DVlsE or sVlsE clones. At day 28 post infection, a time at which spirochetes had been cleared due to a host antibody response, animals were divided into three groups of 4 or 5 mice each and reinfected with either host-adapted WT,DVlsE, or sVlsE via tissue transplantation. Blood samples, ear biopsies and other harvested tissues (heart, bladder, and joint) were collected at indicated time points post transplantation and cultured to monitor the reinfection outcome.

doi:10.1371/journal.pone.0061226.g003

Figure 4. Analysis of B. burgdorferi-specific immune sera by immunoblotting.The whole-cell lysates ofB. burgdorferiWT, sVlsE, andDVlsE clones (106cells/lane) were treated with anti-WT, anti-sVlsE, or anti-DVlsE (panel A, B, and C, respectively) immune sera collected from C3H mice at day 28 post infection. Preimmune sera-treated immunoblot had no immune banding (not shown).

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VlsE is dispensable forB. burgdorferisurvival against passive immunization with T-cell independent antibodies

It has been previously shown that immune sera from Borrelia-infected T-cell deficient mice can protect naı¨ve animals against a challenge withB. burgdorferi[40]. Although our data demonstrate a VlsE requirement for evasion of non-VlsE surface antigens from the host humoral immune response, it is unknown whether VlsE is also important to specifically evade T-cell independent (TI) antibodies. To address this, sera fromBorrelia-infected Hsd:Athy-mic Nude-Foxn1nu(nude) mice lacking functional CD4+and CD8+ T cells was utilized as a source ofBorrelia-specific TI antibodies.

To first determine whether variable VlsE is required to establish persistent infection in nude mice, naı¨ve animals were infected with either host-adapted WT, DVlsE or sVlsE B. burgdorferi clones. Infection was monitored by sampling tissues at day 7, 14, 21, and 42 post infection. All nude mice were successfully infected with each of the differentB. burgdorfericlones as determined by positive blood cultures taken at day 7 post infection (Table 7). Interestingly, all three clones were detectable from ear biopsies collected at day 14 and 21 post infection, indicating a greater ability of theDVlsE and sVlsE clones to persist in nude mice than immunocompetent C3H mice. In contrast to WT, however, DVlsE or sVlsE Table 4.Assessment of reinfection in immunologically VlsE-naı¨ve and VlsE-exposed C3H mice.

Tissue collected (at day post

challenge) DVlsE-cleared C3H mice reinfected witha sVlsE-cleared C3H mice reinfected with

ha WTb

(DVlsE-WT)

haDVlsE (DVlsE-DVlsE)

ha sVlsE (DVlsE -sVlsE)

ha WT (sVlsE-WT)

haDVlsE (sVlsE-DVlsE)

ha sVlsE (sVlsE -sVlsE)

Blood (day 7) 4/4 0/5 0/5 4/4 0/5 0/5

Ear (day 14) 0/4 0/5 0/5 4/4 0/5 0/5

Ear (day 21) 4/4 0/5 0/5 4/4 0/5 0/5

Ear and other tissuesc(day 28) 4/4 0/5 0/5 4/4 0/5 0/5

aValues listed correspond to numbers of cultures positive/numbers tested. bha denotes host-adapted clone.

cOther tissues include heart, bladder and tibiotarsal joint. doi:10.1371/journal.pone.0061226.t004

Figure 5. Experimental design to assay for a VlsE requirement for evasion ofB. burgdorferi-specific antibodies.Immunologically-naı¨ve SCID mice were injected with either WT-specific,DVlsE-specific, or preimmune sera. Mice were divided into groups of 3 animals each and challenged 18 hours later with host-adaptedB. burgdorfericlones. Blood and other tissues were collected at day 7 post challenge and cultured for spirochetes. Group numbers are indicated in the parentheses.

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spirochetes could not be detected in ear tissues by day 42 post infection, suggesting that variable VlsE is required for long-term persistence in this tissue (Table 7). However, mutant spirochetes could be recovered from joint tissues, which suggests that this tissue site in nude mice may provide a protective niche for the VlsE-mutant clones.

To address whether VlsE is important to specifically evade TI antibodies, immunologically-naı¨ve C3H mice were passively immunized with immune sera containing Borrelia-specific TI antibodies and then challenged with either the WT or DVlsE clone (Figure 6). To obtain TI immune sera, nude mice infected with either WT or DVlsE spirochetes were bled at day 14 post infection and sera collected. This time point was chosen to ensure that all nude mice were no older than 8 weeks of age at the time of sera collection; older nude mice have been shown to be somewhat ‘‘leaky’’ and exhibit low-level T cell production [41]. The infection was monitored by culturing blood sampled at day 7 post infection. Consistent with a previous study [40], WT-specific sera was able to prevent infection by in vitro-derived WT spirochetes (Table 8, group 1). In contrast, 3 out of 3 animals that received preimmune sera became infected with thisin vitro-derived WT clone, verifying that these spirochetes were fully infectious at the time of challenge (Table 8, group 2). The total IgM concentration present in the immune sera used above was found to be approximately 38 ng as determined by ELISA, and was utilized in all subsequent experiments described below.

C3H mice that received WT-specific TI sera were also challenged with host-adapted WT (Table 8, group 3), and results show that the immune sera was unable to prevent infection by these spirochetes. Taking into account thatvlsrecombination does not detectably occur duringin vitrocultivation, but SCID-derived

host adapted WT will have experienced some level of vlsE antigenic variation [18], this finding may suggest that variable VlsE is necessary to evade the TI antibody response. Alternatively, low expression of VlsE and/or the presence of other surface antigens normally downregulated in host-adapted spirochetes may explain the inability of in vitro-derived WT B. burgdorferi to successfully challenge TI sera-treated mice. However, both host-adapted andin vitro-derived DVlsE spirochetes were also able to establish infection in mice (Table 8, group 4 and 5) despite the presence of TI immune sera. Together, these findings suggest that VlsE is not necessary forB. burgdorferito survive WT-specific TI antibodies, and that the immune sera contained non-borreliacidal levels of TI antibodies to surface antigens other than VlsE. Moreover, the finding that in vitro-derived WT spirochetes are susceptible to TI antibodies, whilein vitro-derivedDVlsE clones are not, is suggestive that the TI antibody response may be directed mainly to VlsE.

Discussion

Requirement of VlsE for host reinfection

Reinfection byB. burgdorferihas been recognized in both humans and canines [5,13,42,43]. Previous studies using a murine model have demonstrated that cured mice displayed short-term immu-nity to reinfection by tick transmission, intradermalB. burgdorferi inoculation, or with autologous infected tissues [44,45]. It was presumed that because theseB. burgdorferiisolates were autologous, their inability to reinfect was most likely due to a developed immunity to antigenically similar spirochetes. Yet, a contemporary study demonstrated that mice passively immunized toB. burgdorferi were protected againstin vitro-derived spirochetes but susceptible Table 5.Infectivity ofB. burgdorfericlones in passively-immunized SCID mice.

Animal

group# SCID mice injected with

SCID mice

challenged with Organs harvested at day 7 post challengea

Total Blood Heart Ear Bladder Joint

I DVlsE-specific sera WT 3/3 3/3 3/3 0/3 1/3 1/3

II DVlsE-specific sera DVlsE 0/3 0/3 0/3 0/3 0/3 0/3

III DVlsE-specific sera sVlsE 0/3 0/3 0/3 0/3 0/3 0/3

IV WT-specific sera DVlsE 0/3 0/3 0/3 0/3 0/3 0/3

V preimmune sera DVlsE 3/3 3/3 3/3 0/3 0/3 2/3

VI preimmune sera sVlsE 3/3 3/3 3/3 1/3 1/3 2/3

aValues listed correspond to numbers of cultures positive/numbers tested. doi:10.1371/journal.pone.0061226.t005

Table 6.Treatment of infected SCID mice withDVlsE-specific immune sera.

Animal group SCID mice infected with

Immune sera treatment with

(day 4 post transplantation) Blood taken post sera treatment at daya

3 7

A haDVlsEb

DVlsE-specific sera 0/3 0/3

B haDVlsE preimmune sera 3/3 3/3

C ha sVlsE DVlsE-specific sera 1/3 3/3

D ha sVlsE preimmune sera 3/3 3/3

aValues listed correspond to numbers of cultures positive/numbers tested. bha denotes host-adapted clone.

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to challenge by host-adapted spirochetes [37]. Another study showed that mice that had cleared the VlsE-deficientDVlsE clone, and thus were immune to spirochetes antigenically distinct from wild-typeB. burgdorferi, were also resistant to reinfection byin vitro-derived wild-type spirochetes [24]. Because the level of VlsE

expression is substantially greater during murine infection than that ofin vitro-grown spirochetes [35,46], the possibility was raised that the failure to establish host reinfection could potentially be accounted for by a lack of VlsE upregulation [24].

Table 7.Infectivity of host-adapted VlsE mutants in naı¨ve nude mice.

Tissue collected (at day post

infection) Naı¨ve nude mice infected via tissue transplantation witha

ha WTb haDVlsE ha sVlsE

Blood (day 7) 3/3 3/3 3/3

Ear (day 14) 3/3 3/3 2/3

Ear (day 21) 3/3 2/3 1/3

Ear (day 42) 3/3 0/3 0/3

Joint (day 42) 3/3 3/3 3/3

aValues listed correspond to numbers of cultures positive/numbers tested. bha denotes host-adapted clone.

doi:10.1371/journal.pone.0061226.t007

Figure 6. Experimental design to assay for a VlsE requirement for evasion of T-cell independent antibodies.Immunologically-naı¨ve C3H mice were injected with either WT-specific,DVlsE-specific, or preimmune sera originated from nude mice. The sera-treated animals were divided into groups of 3 each and challenged 18 hours post-sera treatment with either host-adapted orin vitro-grownB. burgdorfericlones. Blood and other tissues were harvested at day 7 post challenge and cultured for spirochetes. Group numbers are indicated in the parentheses.

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In the present study, host-adapted clones ofB. burgdorferiwere used in order to eliminate potentially reduced VlsE expression levels that have plagued previous studies. The data presented here demonstrate that host-adapted WT expressing variable VlsE is able to reinfect immunocompetent VlsE-naı¨ve and VlsE-exposed C3H mice. Conversely, aB. burgdorferiVlsE-deficient mutant clone was shown to be unable to reinfect these same mice. The sVlsE clone capable of expressing only a static form of VlsE was also found to be unable to reinfect mice, suggesting that the variable form of VlsE is necessary to allow host reinfection. Finally, passive transfer experiments demonstrated that immune evasion of non-VlsE surface antigens was mediated against hostBorrelia-specific antibodies. Together, the above experiments demonstrate the absolute requirement of variable VlsE for reinfection by the Lyme disease pathogen.

A possible explanation for the inability of the sVlsE clone to reinfect mice is potentially low numbers of VlsE-expressing spirochetes in the transplanted SCID ear tissues. In support of this, the sVlsE clone expressing a static form of VlsE could successfully challenge sera-treated mice, but only after infection was first established (day 4 post infection) presumably because this allowed expansion of VlsE-expressing spirochetes prior to sera treatment. However, an additional factor that may have contrib-uted to the failure of the sVlsE clone to reinfect is delayed and/or low-level expression of VlsE in the murine host. Western blot analysis showed that in vitro-cultured sVlsE mutant spirochetes expressed VlsE at lower levels than those of the wild type (see Fig. 2). Transcriptional regulation is thought to involve the 59 -noncoding region ofvlsEcontaining an inverted DNA repeat that is predicted to form a stable cruciform structure [47]. Though the inverted repeat does not seem to limit access to thevlsEpromoter in vitro [48], it still may be potentially involved in timely transcriptional upregulation ofvlsEin the mammalian host. The vlsE gene copy in our generated sVlsE mutant does not contain this region due to the inherent difficulties in cloning large DNA inverted repeats. Therefore, it is possible that expression of VlsE in the SCID-derived host adapted sVlsE clone remained at insufficient levels for spirochetes to evade an antibody-mediated immune response in order to reinfect C3H mice. Future studies using sVlsE clones containing the full-length inverted DNA repeat sequence will be necessary to address this question.

An alternative explanation for the inability of theDVlsE clone to reinfect mice and resist Borrelia-specific immune sera is the presence of antibodies developed to outer surface protein C (OspC). OspC is an immunodominant lipoprotein whose expres-sion is required for tick-derived or in vitro-grown B. burgdorferito establish infection in vivo [49,50,51,52,53,54]. It has been hypothesized that VlsE may assume an essential, yet unknown

function of OspC [55]. If true, then the expectation would be that VlsE-deficient spirochetes will only survive in mammals if OspC continues to be expressed. Thus, it is conceivable that OspC-specific immunoglobulins could readily eliminate OspC-expressing spirochetes, whereas non-OspC expressing clones simply fail to establish infection due to the absence of OspC and its putative substitute, VlsE. However, this possibility fails to completely explain the inability of the sVlsE clone to reinfect VlsE-naı¨ve mice. Experiments addressing the role of anti-OspC antibodies in this process are currently underway.

VlsE-mediated immune avoidance inB. burgdorferi? The data presented here suggest that variable VlsE is necessary for B. burgdorferi to specifically evade the acquired humoral immune response. Passively-transferred antibodies that were developed to non-VlsE surface antigens and shown to provide immunity against the VlsE-deficient clone, were not borreliacidal to wild-type spirochetes. This VlsE-mediated immune evasion may hint at a possible shielding mechanism that has been previously proposed for preventing other surface antigens of B. burgdorferi from being recognized by borreliacidal antibodies [24,32,33,34]. However, the experiments detailed here do not offer much insight into the mechanistic details of how VlsE may shield surface epitopes. A precedent for potential antibody shielding by B. burgdorferihas been previously demonstrated for the outer surface protein, OspA. This lipoprotein, synthesized in ticks and rarely in mammals [56,57], was shown to limit the access of antibodies to the immunogenic protein P66in vitro [34]. Additionally, a more recent study demonstrated that OspA expressed in feeding ticks blocked recognition of conserved borrelial antigens by host antibodies derived during the uptake of a blood meal [58].

It is also plausible that VlsE could mask surface antigens in association with other molecules. It has been shown that Plasmodium falciparum can evade an immune response through IgM shielding of protective IgG epitopes [59]. Interestingly, the binding of non-specific IgM shielded surface proteins without compromising their function [59]. A similar immunoevasive strategy could conceivably be in place for VlsE-mediated shielding, whereby non-borreliacidal immunoglobulins or other host factor(s) may bind specifically or non-specifically to the highly antigenically variable VlsE protein.

Another possible mechanism of VlsE-mediated immune evasion is linked to the immunodominant nature of this lipoprotein [35]. VlsE may override antibody production that leads to predominant levels of anti-VlsE antibodies and subdominant titers of immuno-globulins to other surface antigens [21]. However, data presented here suggest that VlsE does not suppress production of non-VlsE specific antibodies in the course of an adaptive immune response. Table 8.Infectivity ofB. burgdorfericlones in C3H mice passively immunized with T-cell independent antibodies.

Animal group#

C3H mice injected with immune

sera taken from nude mice C3H mice challenged with Totala

1 WT-specific sera WT 0/4

2 preimmune sera WT 3/3

3 WT-specific sera ha WTb 3/3

4 WT-specific sera haDVlsE 4/4

5 DVlsE-specific sera DVlsE 4/4

aValues listed correspond to numbers of cultures positive/numbers tested. bha denotes host-adapted clone.

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The immune sera generated in immunocompetent mice against wild-typeB. burgdorferi contained non-VlsE specific immunoglob-ulins at levels sufficient enough to prevent infection by theDVlsE clone (see group IV; Table 5). Yet, the findings themselves do not completely exclude an ‘‘overriding’’ mechanism, but instead only argue against such a system for evading an acquired humoral response.

Previous studies have suggested that VlsE may act as a TI antigen [24,33], possibly through direct stimulation of IgM-producing B cell subsets. Therefore, it remains possible that VlsE may function to override TI antibody production during the very early stages of infection. Our data suggest that immune sera derived from nude mice infected with wild-type B. burgdorferi contained subdominant titers of TI antibodies against non-VlsE surface antigens, as shown by their inability to prevent infection by theDVlsE clone. In contrast, the same sera appeared to have anti-VlsE TI antibodies at sufficient levels to prevent infection by in vitro-grown wild-typeB. burgdorferi(Table 7).

In conclusion, the work presented here demonstrates for the first time the absolute requirement of variable VlsE for host reinfection. Moreover, the data suggest that VlsE is specifically involved in evasion of non-VlsE surface antigens from the acquired humoral immune response. Future study into the mechanism behind VlsE-mediated immune avoidance has the potential to reveal how B. burgdorferi resists the robust antibody response elicited against surface antigens other than VlsE. Obtaining such knowledge could significantly improve our understanding of immune evasion by this important pathogen, and may have general implications for other pathogen systems as well.

Materials and Methods

Ethics statement

All experimental procedures involving animals were carried out in accordance with the American Association for Accreditation of Laboratory Animal Care (AAALAC) protocol and the institutional guidelines set by the Office of Campus Veterinarian at Washing-ton State University (Animal Welfare Assurance A3485-01 and USDA registration number 91-R-002). Washington State Univer-sity AAALAC and institutional guidelines are in compliance with the U.S. Public Health Service Policy on Humane Care and Use of Laboratory Animals. All animals were maintained at Washing-ton State University in an AAALAC-accredited animal facility. The Washington State University Institutional Animal Care and Use Committee reviewed and approved the animal protocol associated with the present study.

Murine infection

Male, C3H/HeNHsd (C3H) and Hsd:Athymic Nude-Foxn1nu (nude) mice of 4–6 weeks of age were obtained from Harlan (Indianapolis, IN), and C3SnSmn.CB17-Prkdcscid/J (SCID) mice of 4–5 weeks of age were purchased from Jackson Laboratories (Bar Harbor, ME). C3H, SCID, and nude mice of 5–8 weeks old were challenged through needle inoculation with 16103cells ml21and 16104 cells ml21 via intraperitoneal and subcutaneous routes, respectively. All B. burgdorferi clones harboring recombinant plasmids were cultured in media containing appropriate antibiotic prior to murine infection. B. burgdorfericlones were passaged no more than two timesin vitrofrom frozen glycerol stock prior to use in mouse infection studies.

Alternatively, animals were challenged by tissue transplantation of ears derived from infected SCID mice as previously described [44]. For tissue transplantation, SCID mice were sacrificed at day 28 post challenge and ear pinnae were cut into small, circular

pieces by a sterile ear punch and stored at280uC. Infected ear tissues were thawed on ice as needed and three ear pieces per animal were used for a mouse challenge. Specifically, a skin incision (2–3 mm) was aseptically made in the lumbar region and ear pieces were inserted subcutaneously. The infectivity of tissue-derived spirochetes was tested on naı¨ve C3H mice (Table 3). To verify infection, 50 ul of blood was aseptically drawn from a mouse via maxillary bleed at day 4 or 7 post challenge and cultured in 3 ml of BSK-II containing Borrelia antibiotic cocktail (0.02 mg ml21 phosphomycin, 0.05 mg ml21 rifampicin and 2.5 mg ml21 amphotericin B). To monitor the progress of infection, ear, heart, bladder, and joint tissues were aseptically harvested at various time points post challenge and cultured in 1.0 ml of BSK-II supplemented with the antibiotic cocktail. Dark-field microscopy was used to confirm the presence of viable spirochetes for each cultured tissue. For each use, infected ear tissue was tested for the presence of viable borrelial cells by culture.

Bacterial strains

Borrelia burgdorferi strain B31-A3 (WT) was kindly provided by Patti Rosa. B31-A3Dvls(DVlsE) was generated in a previous study [24], and was a generous gift from George Chaconas. All B. burgdorfericlones were cultivated in liquid Barbour–Stoenner–Kelly II media (BSK-II) supplemented with 6% rabbit serum (Cedarlane Laboratories, Burlington, NC) and incubated at 35uC.

Plasmid construction

To obtain the B. burgdorferi lp28-1Dvls::vlsE clone (sVlsE), a targeted deletion plasmid, pAR2, was generated. The target region identical to DNA basepair coordinates 17,296 to 18,800 on lp28-1 was PCR amplified using the P266 (CCGGGGTACCGCTGTA-TAATGTC AAATGGCTAGG) and P267 (GTGCCGCTCGA-GAGGCTGCTGATGAGGCGAG) primers. The amplicon was cloned into pJET1.2 vector using CloneJET PCR Cloning Kit (Fermentas, USA). The target sequence was then recovered by digestion with KpnI and XhoI, followed by cloning into pTB44 [24] to generate pAR1. pTB44 contains aflgBp-drivenkangene and a 70 bp replicated telomere from the left end of lp17. ThevlsE expression site with native promoter was PCR amplified from pMBL20 (a gift from Steven Norris; [23]) using the P260 (GGTCTAGAAGAAATGAAAAATTCTCTCACCTACACTT)

and P261 (GCCGGCCGGAGGG

CATAGTCGTGTCCA-TACA) primers, and then cloned into pJET1.2. The vlsE insert was recovered by digestion with EagI and XbaI and cloned into pAR1.

B. burgdorferitransformation

B. burgdorfericells were electroporated with pAR2 as previously described [24]. After electroporation with a total of 50 ug of DNA, spirochetes were resuspended in 10 ml prewarmed BSK-II media. Cells were recovered at 35uC for 24 hr and then diluted in 100 ml of pre-warmed BSK-II supplemented with 200 ug ml21

kanamy-cin. The transformed cell suspension was aliquoted into 96-well plates and incubated at 35uC for 3–4 weeks. DNA from positive wells was extracted using a DNeasy Blood and Tissue Kit (Qiagen, Germantown, MD), and used for PCR analysis to confirm the presence of the kanamycin-resistance gene and vlsE utilizing

P54/55 (CATATGAGCCATATTCAACGGGAAACG and

AAAGCCGTTTCTGTAA TGAAGGAG) and P243/244

(GCGATATAAGTAGTACGACGGGGAAACCAG and

CAAGGC AGGAGGTGTTTCTTTACTAGCAGC) primer

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Field inversion gel electrophoresis

Plasmid DNA fromB. burgdorferi transformations was purified utilizing the Qiagen Plasmid Midi Kit (Qiagen, Germantown, MD). Approximately 450 ng of DNA was separated on a 0.65% Seakem agarose gel at 80 V for 40 min, followed by initiation of Program 0 on an MJ Research PPI-200 programmable power inverter (kindly provided by D. Scott Samuels) at 80 V for 21 hr with buffer recirculation [60].

Immunoblotting

B. burgdorfericlones were grown in BSK-II to the late stationary phase. Cells were counted, pelleted by centrifugation at 6,0006g for 10 min at 4uC, and then washed twice with ice-cold PBS. After removal of PBS, the cells were suspended in sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis sample buffer (100 mM Tris [pH 6.8], 2% SDS, 5% b-mercaptoethanol, 10% glycerol, 0.01% bromophenol blue), and incubated at 95uC for 10 min. Approximately 16106or 16108cells were loaded to each sample lane of 15% acrylamide minigel (see SDS-PAGE analysis in Figure S1). Resolved proteins were transferred onto poly-vinylidene fluoride (PVDF) membrane with a pore size of 0.45 um (Immobilon-P, Millipore, USA). The blot was blocked with 5% nonfat dry milk in PBS for 18 hr at 4uC and then incubated in the same solution supplemented with either 1:1,000 diluted rabbit anti-FlaB antibody (Rockland Immunochemicals, Gilbertsville, PA), 1:2,000 diluted rabbit anti-C6serum (generously provided by

Mario Philipp), or 1:1,000 diluted mouse antiWT, sVlsE, or -DVlsE immune, or preimmune sera for 1 hr. To generate anti-WT, -sVlsE, or -DVlsE immune sera, naı¨ve C3H mice (3 mice per group) were infected with WT, sVlsE, or DVlsE (1.16104 cells ml21) via needle inoculation. At day 28 post infection blood was collected and equal amount of immune sera derived from animals of the same group were pooled and filter-sterilized by passage through 0.22 um syringe filter. Preimmune sera were collected from three naı¨ve C3H mice.

After 4 washes of 10 min each with TBST, the primary antibodies were detected utilizing donkey rabbit or anti-mouse HorseRadish Peroxidase (HRP)-conjugated secondary antibody (Jackson ImmunoResearch Laboratories, West Grove, PA) diluted to 1:5,000 and 1:1,000, respectively, in TBST for 30 min. The blot was washed 3 times in TBST for 10 min each, followed by a last wash in nano-pure water. The blots were visualized on Enhanced ChemiLuminescence (ECL) development. Surface proteolysis involving proteinase K digestion of intact spirochetes was performed as previously described [61].

Passive immunization of mice

To obtain immune sera, C3H and nude mice were infected with B. burgdorferithrough needle inoculation or tissue transplantation as described above. Blood from isoflurane-euthanized, infected C3H and nude mice were collected via cardiac puncture at day 21 and 14 post infection, respectively. Approximately, 600–900 ul of immune serum was collected from each mouse. Collected blood was kept at room temperature for 30 min and then centrifuged at 6,0006g for 15 min. Sera were removed from the blood cell pellet and stored at 220uC until required for passive immunization. Immune sera were thawed on ice immediately before use and pooled if obtained from mice infected with the same clone. Sera were then diluted to 1:3 with sterile saline to minimize a loss associated with sterilization and immunization. Diluted sera were filter-sterilized by passage through 0.22 um syringe filter. The mice to be passively immunized were injected with total of 300 ul of diluted immune sera. IgM titer was measured by a mouse IgM ELISA according to the manufacturer’s instruction (Immunology Consultant Laboratory, OR). B. burgdorferi-specific sera derived from nude mice at day 14 post infection contained 377 ng/ml of IgM.

Supporting Information

Figure S1 SDS-PAGE analysis of whole-cell lysates ofB. burgdorfericlones. WT, sVlsE, and DVlsE whole-cell lysates (106cells/lane) were subjected to electrophoresis in a 15% sodium dodecyl sulfate polyacrylamide gel under reducing conditions. Electrophoresis was carried out in Tris-glycine buffer containing 0.01% SDS. The slab gel was stained with Coomassie Blue R-250 and destained with methanol:water:acetic acid (5:4:1, v/v). (TIF)

Acknowledgments

The authors thank Tim Casselli, Allison James, Petronella Hove, and Yvonne Tourand for critical reading of the manuscript.

Author Contributions

Conceived and designed the experiments: ASR TB. Performed the experiments: ASR. Analyzed the data: ASR TB. Contributed reagents/ materials/analysis tools: TB. Wrote the paper: ASR TB.

References

1. Barbour AG (2001) Borrelia: a diverse and ubiquitous genus of tick-borne pathogens. In: Scheld MW, Craig WA, Hughes JM, editors. Emerging Infections 5. Washington, D.C.: American Society for Microbiology. pp. 153–173. 2. Steere AC, Coburn J, Glickstein L (2004) The emergence of Lyme disease. J Clin

Invest 113: 1093–1101.

3. Radolf JD, Caimano MJ, Stevenson B, Hu LT (2012) Of ticks, mice and men: understanding the dual-host lifestyle of Lyme disease spirochaetes. Nat Rev Microbiol 10: 87–99.

4. Steere AC (2001) Lyme disease. N Engl J Med 345: 115–125.

5. Krause PJ, Foley DT, Burke GS, Christianson D, Closter L, et al. (2006) Reinfection and relapse in early Lyme disease. Am J Trop Med Hyg 75: 1090– 1094.

6. Nowakowski J, Nadelman RB, Sell R, McKenna D, Cavaliere LF, et al. (2003) Long-term follow-up of patients with culture-confirmed Lyme disease. Am J Med 115: 91–96.

7. Nowakowski J, Schwartz I, Nadelman RB, Liveris D, Aguero-Rosenfeld M, et al. (1997) Culture-confirmed infection and reinfection withBorrelia burgdorferi. Ann Intern Med 127: 130–132.

8. Salazar JC, Gerber MA, Goff CW (1993) Long-term outcome of Lyme disease in children given early treatment. J Pediatr 122: 591–593.

9. Smith RP, Schoen RT, Rahn DW, Sikand VK, Nowakowski J, et al. (2002) Clinical characteristics and treatment outcome of early Lyme disease in patients with microbiologically confirmed erythema migrans. Ann Intern Med 136: 421– 428.

10. Weber K, Schierz G, Wilske B, Neubert U, Krampitz HE, et al. (1986) Reinfection in erythema migrans disease. Infection 14: 32–35.

11. Wormser GP, Ramanathan R, Nowakowski J, McKenna D, Holmgren D, et al. (2003) Duration of antibiotic therapy for early Lyme disease. A randomized, double-blind, placebo-controlled trial. Ann Intern Med 138: 697–704. 12. Nadelman RB, Wormser GP (2007) Reinfection in patients with Lyme disease.

Clin Infect Dis 45: 1032–1038.

13. Golde WT, Robinson-Dunn B, Stobierski MG, Dykhuizen D, Wang IN, et al. (1998) Culture-confirmed reinfection of a person with different strains ofBorrelia burgdorferisensu stricto. J Clin Microbiol 36: 1015–1019.

14. Norris SJ (2006) Antigenic variation with a twist - the Borreliastory. Mol Microbiol 60: 1319–1322.

(12)

16. Zhang JR, Hardham JM, Barbour AG, Norris SJ (1997) Antigenic variation in Lyme disease borreliae by promiscuous recombination of VMP-like sequence cassettes. Cell 89: 275–285.

17. Zhang JR, Norris SJ (1998) Genetic variation of theBorrelia burgdorferigenevlsE

involves cassette-specific, segmental gene conversion. Infect Immun 66: 3698– 3704.

18. Zhang JR, Norris SJ (1998) Kinetics and in vivo induction of genetic variation of

vlsEinBorrelia burgdorferi. Infect Immun 66: 3689–3697.

19. Labandeira-Rey M, Skare JT (2001) Decreased infectivity inBorrelia burgdorferi

strain B31 is associated with loss of linear plasmid 25 or 28-1. Infect Immun 69: 446–455.

20. Purser JE, Norris SJ (2000) Correlation between plasmid content and infectivity inBorrelia burgdorferi. Proc Natl Acad Sci U S A 97: 13865–13870.

21. Labandeira-Rey M, Seshu J, Skare JT (2003) The absence of linear plasmid 25 or 28-1 ofBorrelia burgdorferidramatically alters the kinetics of experimental infection via distinct mechanisms. Infect Immun 71: 4608–4613.

22. Purser JE, Lawrenz MB, Caimano MJ, Howell JK, Radolf JD, et al. (2003) A plasmid-encoded nicotinamidase (PncA) is essential for infectivity ofBorrelia burgdorferiin a mammalian host. Mol Microbiol 48: 753–764.

23. Lawrenz MB, Wooten RM, Norris SJ (2004) Effects ofvlsEcomplementation on the infectivity of Borrelia burgdorferilacking the linear plasmid lp28-1. Infect Immun 72: 6577–6585.

24. Bankhead T, Chaconas G (2007) The role of VlsE antigenic variation in the Lyme disease spirochete: persistence through a mechanism that differs from other pathogens. Mol Microbiol 65: 1547–1558.

25. Kenedy MR, Lenhart TR, Akins DR (2012) The role ofBorrelia burgdorferiouter surface proteins. FEMS Immunol Med Microbiol.

26. Brisson D, Drecktrah D, Eggers CH, Samuels DS (2012) Genetics ofBorrelia burgdorferi. Annu Rev Genet 46: 515–536.

27. Coutte L, Botkin DJ, Gao L, Norris SJ (2009) Detailed analysis of sequence changes occurring duringvlsEantigenic variation in the mouse model ofBorrelia burgdorferiinfection. PLoS Pathog 5: e1000293.

28. Embers ME, Liang FT, Howell JK, Jacobs MB, Purcell JE, et al. (2007) Antigenicity and recombination of VlsE, the antigenic variation protein of

Borrelia burgdorferi, in rabbits, a host putatively resistant to long-term infection with this spirochete. FEMS Immunol Med Microbiol 50: 421–429.

29. McDowell JV, Sung SY, Hu LT, Marconi RT (2002) Evidence that the variable regions of the central domain of VlsE are antigenic during infection with Lyme disease spirochetes. Infect Immun 70: 4196–4203.

30. Indest KJ, Howell JK, Jacobs MB, Scholl-Meeker D, Norris SJ, et al. (2001) Analysis ofBorrelia burgdorferi vlsEgene expression and recombination in the tick vector. Infect Immun 69: 7083–7090.

31. Ohnishi J, Schneider B, Messer WB, Piesman J, de Silva AM (2003) Genetic variation at thevlsElocus ofBorrelia burgdorferiwithin ticks and mice over the course of a single transmission cycle. J Bacteriol 185: 4432–4441.

32. Liang FT, Jacobs MB, Bowers LC, Philipp MT (2002) An immune evasion mechanism for spirochetal persistence in Lyme borreliosis. J Exp Med 195: 415– 422.

33. Philipp MT, Bowers LC, Fawcett PT, Jacobs MB, Liang FT, et al. (2001) Antibody response to IR6, a conserved immunodominant region of the VlsE lipoprotein, wanes rapidly after antibiotic treatment ofBorrelia burgdorferiinfection in experimental animals and in humans. J Infect Dis 184: 870–878. 34. Bunikis J, Barbour AG (1999) Access of antibody or trypsin to an integral outer

membrane protein (P66) ofBorrelia burgdorferiis hindered by Osp lipoproteins. Infect Immun 67: 2874–2883.

35. Liang FT, Yan J, Mbow ML, Sviat SL, Gilmore RD, et al. (2004)Borrelia burgdorferichanges its surface antigenic expression in response to host immune responses. Infect Immun 72: 5759–5767.

36. Barthold SW (1999) Specificity of infection-induced immunity amongBorrelia burgdorferisensu lato species. Infect Immun 67: 36–42.

37. de Silva AM, Fikrig E, Hodzic E, Kantor FS, Telford SR, 3rd, et al. (1998) Immune evasion by tickborne and host-adaptedBorrelia burgdorferi. J Infect Dis 177: 395–400.

38. Elias AF, Stewart PE, Grimm D, Caimano MJ, Eggers CH, et al. (2002) Clonal polymorphism ofBorrelia burgdorferistrain B31 MI: implications for mutagenesis in an infectious strain background. Infect Immun 70: 2139–2150.

39. Purser JE, Norris SJ (2000) Correlation between plasmid content and infectivity inBorrelia burgdorferi. Proc Natl Acad Sci U S A 97: 13865–13870.

40. McKisic MD, Barthold SW (2000) T-cell-independent responses to Borrelia burgdorferiare critical for protective immunity and resolution of lyme disease. Infect Immun 68: 5190–5197.

41. MacDonald HR, Lees RK, Sordat B, Zaech P, Maryanski JL, et al. (1981) Age-associated increase in expression of the T cell surface markers Thy-1, Lyt-1, and Lyt-2 in congenitally athymic (nu/nu) mice: analysis by flow microfluorometry. J Immunol 126: 865–870.

42. Kalish RA, McHugh G, Granquist J, Shea B, Ruthazer R, et al. (2001) Persistence of immunoglobulin M or immunoglobulin G antibody responses to

Borrelia burgdorferi10–20 years after active Lyme disease. Clin Infect Dis 33: 780– 785.

43. Hovius KE, Rijpkema SG, Westers P, van der Zeijst BA, van Asten FJ, et al. (1999) A serological study of cohorts of young dogs, naturally exposed toIxodes ricinusticks, indicates seasonal reinfection byBorrelia burgdorferisensu lato. Vet Q 21: 16–20.

44. Barthold SW (1993) Antigenic stability of Borrelia burgdorferiduring chronic infections of immunocompetent mice. Infect Immun 61: 4955–4961. 45. Piesman J, Dolan MC, Happ CM, Luft BJ, Rooney SE, et al. (1997) Duration of

immunity to reinfection with tick-transmitted Borrelia burgdorferi in naturally infected mice. Infect Immun 65: 4043–4047.

46. Crother TR, Champion CI, Wu XY, Blanco DR, Miller JN, et al. (2003) Antigenic composition ofBorrelia burgdorferiduring infection of SCID mice. Infect Immun 71: 3419–3428.

47. Hudson CR, Frye JG, Quinn FD, Gherardini FC (2001) Increased expression of

Borrelia burgdorferi vlsEin response to human endothelial cell membranes. Mol Microbiol 41: 229–239.

48. Bykowski T, Babb K, von Lackum K, Riley SP, Norris SJ, et al. (2006) Transcriptional regulation of theBorrelia burgdorferiantigenically variable VlsE surface protein. J Bacteriol 188: 4879–4889.

49. Wilske B, Preac-Mursic V, Jauris S, Hofmann A, Pradel I, et al. (1993) Immunological and molecular polymorphisms of OspC, an immunodominant major outer surface protein ofBorrelia burgdorferi. Infect Immun 61: 2182–2191. 50. Grimm D, Tilly K, Byram R, Stewart PE, Krum JG, et al. (2004) Outer-surface protein C of the Lyme disease spirochete: a protein induced in ticks for infection of mammals. Proc Natl Acad Sci U S A 101: 3142–3147.

51. Stewart PE, Wang X, Bueschel DM, Clifton DR, Grimm D, et al. (2006) Delineating the requirement for theBorrelia burgdorferivirulence factor OspC in the mammalian host. Infect Immun 74: 3547–3553.

52. Tilly K, Krum JG, Bestor A, Jewett MW, Grimm D, et al. (2006)Borrelia burgdorferi OspC protein required exclusively in a crucial early stage of mammalian infection. Infect Immun 74: 3554–3564.

53. Xu Q, Seemanapalli SV, McShan K, Liang FT (2006) Constitutive expression of outer surface protein C diminishes the ability ofBorrelia burgdorferi to evade specific humoral immunity. Infect Immun 74: 5177–5184.

54. Pal U, Yang X, Chen M, Bockenstedt LK, Anderson JF, et al. (2004) OspC facilitatesBorrelia burgdorferiinvasion ofIxodes scapularissalivary glands. J Clin Invest 113: 220–230.

55. Tilly K, Bestor A, Dulebohn DP, Rosa PA (2009) OspC-independent infection and dissemination by host-adaptedBorrelia burgdorferi. Infect Immun 77: 2672– 2682.

56. Barthold SW, Fikrig E, Bockenstedt LK, Persing DH (1995) Circumvention of outer surface protein A immunity by host-adapted Borrelia burgdorferi. Infect Immun 63: 2255–2261.

57. Schwan TG, Piesman J, Golde WT, Dolan MC, Rosa PA (1995) Induction of an outer surface protein onBorrelia burgdorferiduring tick feeding. Proc Natl Acad Sci U S A 92: 2909–2913.

58. Battisti JM, Bono JL, Rosa PA, Schrumpf ME, Schwan TG, et al. (2008) Outer surface protein A protects Lyme disease spirochetes from acquired host immunity in the tick vector. Infect Immun 76: 5228–5237.

59. Barfod L, Dalgaard MB, Pleman ST, Ofori MF, Pleass RJ, et al. (2011) Evasion of immunity toPlasmodium falciparummalaria by IgM masking of protective IgG epitopes in infected erythrocyte surface-exposed PfEMP1. Proc Natl Acad Sci U S A 108: 12485–12490.

60. Chaconas G, Stewart PE, Tilly K, Bono JL, Rosa P (2001) Telomere resolution in the Lyme disease spirochete. EMBO J 20: 3229–3237.

Imagem

Figure 2. Expression and surface localization of VlsE by B.
Table 5), demonstrating that these clones were fully capable of infecting mice. Together, these data support the findings of our reinfection experiments, emphasizing the importance of variable VlsE for B
Table 6). Overall, these data suggest that static VlsE can provide some measure of immune avoidance for non-VlsE surface antigens, but only after infection is established.
Figure 5. Experimental design to assay for a VlsE requirement for evasion of B. burgdorferi -specific antibodies
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